Variant #0000511853 (NC_000002.11:g.179466443G>C, NM_001267550.1:c.55374C>G (TTN))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.179466443G>C
DNA change (hg38) g.178601716G>C
Published as TTN(NM_001256850.1):c.50451C>G (p.(Ser16817Arg)), TTN(NM_001267550.1):c.55374C>G (p.S18458R), TTN(NM_001267550.2):c.55374C>G (p.S18458R), TTN(NM_1...)
ISCN -
DB-ID TTN_003780 See all 8 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0004 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTN NM_001267550.1 ?/. - c.55374C>G r.(?) p.(Ser18458Arg)
TTN-AS1 NR_038272.1 ?/. - n.3917+1049G>C r.(?) -


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